Detalhe da pesquisa
1.
Cell lineage-specific mitochondrial resilience during mammalian organogenesis.
Cell
; 186(6): 1212-1229.e21, 2023 03 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-36827974
2.
Balancing of mitochondrial translation through METTL8-mediated m3C modification of mitochondrial tRNAs.
Mol Cell
; 81(23): 4810-4825.e12, 2021 12 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-34774131
3.
YbeY is required for ribosome small subunit assembly and tRNA processing in human mitochondria.
Nucleic Acids Res
; 49(10): 5798-5812, 2021 06 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-34037799
4.
Regulation of Mammalian Mitochondrial Gene Expression: Recent Advances.
Trends Biochem Sci
; 42(8): 625-639, 2017 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-28285835
5.
Variants in PUS7 Cause Intellectual Disability with Speech Delay, Microcephaly, Short Stature, and Aggressive Behavior.
Am J Hum Genet
; 103(6): 1045-1052, 2018 12 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-30526862
6.
METTL15 introduces N4-methylcytidine into human mitochondrial 12S rRNA and is required for mitoribosome biogenesis.
Nucleic Acids Res
; 47(19): 10267-10281, 2019 11 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-31665743
7.
NSUN2 introduces 5-methylcytosines in mammalian mitochondrial tRNAs.
Nucleic Acids Res
; 47(16): 8720-8733, 2019 09 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-31276587
8.
Reconstruction of the Proximal Scaphoid With a Medial Femoral Trochlea Osteochondral Graft: Minimum 2-Year Results.
J Hand Surg Am
; 46(3): 248.e1-248.e9, 2021 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-33257054
9.
TRMT2B is responsible for both tRNA and rRNA m5U-methylation in human mitochondria.
RNA Biol
; 17(4): 451-462, 2020 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-31948311
10.
Mutations in ELAC2 associated with hypertrophic cardiomyopathy impair mitochondrial tRNA 3'-end processing.
Hum Mutat
; 40(10): 1731-1748, 2019 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-31045291
11.
Human mitochondrial ribosomes can switch their structural RNA composition.
Proc Natl Acad Sci U S A
; 113(43): 12198-12201, 2016 10 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-27729525
12.
The Pseudouridine Synthase RPUSD4 Is an Essential Component of Mitochondrial RNA Granules.
J Biol Chem
; 292(11): 4519-4532, 2017 03 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-28082677
13.
TRMT5 Mutations Cause a Defect in Post-transcriptional Modification of Mitochondrial tRNA Associated with Multiple Respiratory-Chain Deficiencies.
Am J Hum Genet
; 97(2): 319-28, 2015 Aug 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-26189817
14.
Mutations in GTPBP3 cause a mitochondrial translation defect associated with hypertrophic cardiomyopathy, lactic acidosis, and encephalopathy.
Am J Hum Genet
; 95(6): 708-20, 2014 Dec 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-25434004
15.
New insights into the phenotype of FARS2 deficiency.
Mol Genet Metab
; 122(4): 172-181, 2017 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-29126765
16.
Mutations in the mitochondrial cysteinyl-tRNA synthase gene, CARS2, lead to a severe epileptic encephalopathy and complex movement disorder.
J Med Genet
; 52(8): 532-40, 2015 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-25787132
17.
Two siblings with homozygous pathogenic splice-site variant in mitochondrial asparaginyl-tRNA synthetase (NARS2).
Hum Mutat
; 36(2): 222-31, 2015 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-25385316
18.
Mitochondrial transcript maturation and its disorders.
J Inherit Metab Dis
; 38(4): 655-80, 2015 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-26016801
19.
VARS2 and TARS2 mutations in patients with mitochondrial encephalomyopathies.
Hum Mutat
; 35(8): 983-9, 2014 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-24827421
20.
A library of base editors for the precise ablation of all protein-coding genes in the mouse mitochondrial genome.
Nat Biomed Eng
; 7(5): 692-703, 2023 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-36470976